regulation of spermatogenesis by crem
| PAG Title | regulation of spermatogenesis by crem |
| PAG ID | WAG000830 |
| Type | P |
| Source Link |  BioCarta |
| Publication Reference | NA |
| PAG Description | The transcriptiol regulator CREM plays a key role in spermatogenesis, acting as a central transcription factor triggering a cascade of transcriptiol activation of post-meiotic genes involved in this process such as calspermin and testis angiotensin-converting enzyme. The key role of CREM in sperm formation is demonstrated by the male sterility of mice lacking CREM, the failure of spermatids to develop into mature sperm, and a lack of post-meiotic gene expression in these animals. Prior to meiosis, splice variants of CREM act as antagonists of cAMP-dependent transcriptiol activation, but coordite with spermatogenesis, the potent transcriptiol activator CREM tau splice variant is highly expressed. In other tissues CREM activates genes in response to cAMP through phosphorylation and CBP association, but transcriptiol activation by CREM in male germ cells is CBP independent. Stimulation of spermatids with follicle-stimulating hormone (FSH) induces cAMP formation, and the association of CREM with the coactivator ACT, although the mechanism regulating the interaction of CREM with ACT is not yet known. A two-hybrid screen looking for ACT interacting factors revealed another surprising component regulating CREM, the kinesin Kif17b. Kinesins are molecular motors that interact with microtubules to transport organelles and other material within the cell. Kif17b is actively exported from the nucleus in a Crm1-dependent manner, so when it is bound to ACT the export of Kif17b excludes CREM-ACT from the nucleus and blocks transcriptiol activation by this complex. The mechanism regulating the interaction of Kif17b with ACT to drive CREM activation is not yet known. Although the regulation of transcription by a kinesin is surprising, a functiol connection between cytoskeletal elements and transcriptiol regulation is not unprecedented, as demonstrated by the transcription factor MIZ-1 that regulates transcription in response to changes in microtubule structure. |
| Species | Homo sapiens |
| Quality Metric Scores | nCoCo Score: 400 |
| Information Content | Rich |
| Other IDs | |
| Base PAG ID | WAG000830 |
| Human Phenotyte Annotation | |
| Curator | PAGER curation team |
| Curator Contact | PAGER-contact@googlegroups.com |
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